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. 2019 Mar 1;9(3):545–556. doi: 10.1016/j.apsb.2019.02.009

Table 3.

1H NMR spectroscopic data (δ) for compounds 15 and 16a (δ in ppm, J in Hz).

No. 15 16 No. 15 16
1 6.24 s 6.27 s 19 3.06 d (19.0), 2.35 d (19.0) 3.64 d (19.0), 2.60 d (19.0)
4 1.48 m 1.72 m 21 7.24 s 7.26 s
5 1.90 (overlapped) 2.48 m 22 6.26 s 7.28 s
6a 1.91 m 2.73 t (14.5) 23 7.37 s 7.38 s
6b 1.67 m 2.44 m
7 3.95 t (3.0) 28 0.87 d (7.0) 0.90 d (7.0)
9 2.68 d (6.5) 2.20 d (4.5) 29 0.80 d (7.0) 0.86 d (7.0)
11 4.57 td (9.0, 6.0) 4.34 m 30 1.32 s 1.63 s
12a 2.67 dd (13.5, 9.0) 2.80 dd (14.0, 8.5) 3′ 7.16 m
12b 1.33 (overlapped) 1.69 dd (13.5, 6.5)
15 5.69 brd d (3.0) 6.28 brd s 4′ 1.91 s
16a 2.55 ddd (15.5, 11.0, 2.0) 2.58 (overlapped) 5′ 1.88 dd (7.0,1.5)
16b 2.48 ddd (15.5, 7.0, 3.0) 2.42 (overlapped)
17 2.87 dd (11.0, 7.5) 2.92 dd (11.0,7.0) OAc 1.90 s
18 0.81 s 0.86 s
a

NMR data (δ) were measured at 500 MHz in CDCl3 for 15 and 16.